Actively Recruiting

Age: 18Years +
All Genders
NCT02818517

Evaluation and Management of Cardio Toxicity in Oncologic Patients

Led by Tel-Aviv Sourasky Medical Center · Updated on 2022-02-02

1000

Participants Needed

1

Research Sites

804 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The survival rate of cancer patients has greatly increased over the past decades' mainly due to early detection and the use of new medications with higher doses and combined protocols. This achievement comes with the price of cardio toxicity, leading to cardiac dysfunction ranged from transient asymptomatic left ventricular dysfunction to cardiac death. In the long term, the risk of death from cardiovascular causes exceeds that of tumor recurrence for many types of cancer. As a result of the increasing number of long-term cancer survivors the magnitude of this problem is growing. Early identification of cardio toxicity can be identified by clinical follow-up and the use of electrocardiography, cardiac biomarkers (Troponin, brain natriuretic peptide) and echocardiogram. Past studies imply that the addition of angiotensin-converting-enzyme inhibitor (ACE inhibitor) and beta blockers to the patient's treatment may prevent the development of cardiac dysfunction. However, currently there are no specific or clear guidelines for the follow-up and management of cardio-toxicity in cancer patients. The aim of the study: To try to identify who are the patients at increased risk for developing cardio toxicity, by follow up of clinical evaluation, cardiac biomarkers and echocardiogram examination, in purpose of early diagnosis, management and prevention of cardiac events. For achieving this the investigators will build a registry which will include all the oncologic patients going an evaluation in the cardio-oncology clinic in the Tel Aviv Medical Center .

CONDITIONS

Official Title

Evaluation and Management of Cardio Toxicity in Oncologic Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients evaluated in the cardio-oncology clinic in Tel Aviv Medical Center
Not Eligible

You will not qualify if you...

  • Patients in the prospective study who do not sign an informed consent form
  • Patients who choose to stop participating in the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Tel Aviv Medical Center

Tel Aviv, Israel

Actively Recruiting

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Research Team

M

Michal Laufer Perl, MD

CONTACT

U

Udi Chorin, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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